csc
csc

Project Management

The role of the Project Manager is
critical to the success of every
clinical trial

Project Management

Clinical Monitoring

Our Clinical Research Associates (CRAs)
are highly qualified and
industry recognized

Clinical Monitoring

Regulatory Affairs

CSC Ltd. takes pride in submitting
excellent IRB submissions.
Our careful attention to detail

Regulatory Affairs

Our Services

CSC Ltd. provides the following services to pharmaceutical and biotechnology companies:

  • Clinical trial management
  • IRB and MOH submissions and maintenance
  • Collaborative interaction with regulatory authorities and IRBs
  • Investigator site selection and feasibility assessments
  • Contract and budget preparation, negotiation and administration
  • Investigator meeting organization
  • Site training
  • CRA resourcing, mentoring and co-monitoring support
  • Monitoring report review
  • SAE reporting coordination
  • Coordination of site/ vendor/ client communications

 

Feasibility

Our study feasibility assessment process is efficient in identifying the best investigative sites to conduct a clinical trial in Israel.

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Project Management

The role of the Project Manager is critical to the success of every clinical trial. As the primary point person, the PM is responsible for overseeing all client/CRO interactions, managing study sites, coordinating investigator payments, monitoring study metrics, training, assuring adherence to timelines, and coordinating

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Clinical Monitoring

Our Clinical Research Associates (CRAs) are appropriately qualified and industry recognized for their outstanding reputation in customer service, in-depth knowledge of GCP guidelines, regulatory requirements and therapeutic knowledge.

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Investigator Meetings Organization

CSC Ltd. prepares and holds investigator meetings across Israel. Our experience allows us to ensure to our sponsor perfect quality and professionalism of such events

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Regulatory Affairs

CSC Ltd. takes pride in submitting excellent IRB submission. Our careful attention to detail and an excellent relationship with the regulatory authorities helps to expedite the regulatory review process and to shorten drug development timelines.

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Affiliated Services

CSC Clinical Research is able to offer clients additional capabilities by augmenting our in-house services with those of our affiliated partners to be able to provide: Central Laboratory Services, Data Management, Translation Services and Pharmaceutical Distribution.

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